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nsv7072535

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 17 studies. See in: genome view    
    Submitted genomic32,763,548-32,763,643Question Mark
    Overlapping variant regions from other studies: 89 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):31,090,566-31,090,661Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072535Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1732,763,54832,763,643
    nsv7072535RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1731,090,56631,090,661

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757174inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757174Submitted genomicNC_000017.11:g.327
    63548_32763643inv
    GRCh38 (hg38)NC_000017.11Chr1732,763,54832,763,643
    nssv18757174RemappedPerfectNC_000017.10:g.310
    90566_31090661inv
    GRCh37.p13First PassNC_000017.10Chr1731,090,56631,090,661

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv18757174<0.00177266492
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